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抗血管生成疗法能否预防晚期肾细胞癌的脑转移?

Do anti-angiogenic therapies prevent brain metastases in advanced renal cell carcinoma?

作者信息

Vanhuyse Marie, Penel Nicolas, Caty Armelle, Fumagalli Ingrid, Alt Marie, Zini Laurent, Adenis Antoine

机构信息

Centre Oscar-Lambret, 3, rue Frédéric-Combemale, 59020 Lille, France.

出版信息

Bull Cancer. 2012 Dec;99(12):100-6. doi: 10.1684/bdc.2012.1672.

Abstract

BACKGROUND

We analyzed renal cell carcinoma (RCC) brain metastasis (BM) risk factors and compared BM occurrence in metastatic RCC (mRCC) treated with or without anti-angiogenic agents (AA).

METHODS

Data from all consecutive metastatic RCC patients (patients) treated in a french cancer center between 1995 and 2008 were reviewed. Patients had histologically confirmed advanced RCC without synchronous BM at the time of metastasis diagnosis. AA were sorafenib, sunitinib and bevacizumab. We also included patients treated with mTor inhibitors, temsirolimus and everolimus, as they also demonstrated anti-angiogenic activities. Characteristics of the two groups treated with or without AA were compared with a Fisher exact test. Impact of AA on overall survival (OS) and cumulative rate of brain metastasis (CRBM) was explored by Kaplan-Meier method.

RESULTS

One hundred and ninety-nine patients with advanced RCC were identified, 51 treated with AA and 148 without AA. The median follow-up duration was 40 months. BM occurred in 35 patients. Characteristics between AA treated and non-AA treated groups were unbalanced and favoring better prognostic factors in AA treated group. Median OS was 24 months. AA treatment was not associated with a lower CRBM (HR = 0.58 [0.26-1.30], P = 0.187). Median survival free of BM was 11.8 months, CI95% (4.95-18.65) in the group without AA treatment and 28.9 months in the AA group, CI95% (18.64-39.16). Alkaline phosphatase (AP) was an independent prognostic factor for BM (P = 0.05). In multivariate Cox model, after adjustment to AP, AA did not improve the CRBM (aHR = 0.53 [0.22-1.32]).

CONCLUSION

In this retrospective study, AA did not decrease significantly the CRBM. Elevated AP was a predictive factor for BM in mRCC.

摘要

背景

我们分析了肾细胞癌(RCC)脑转移(BM)的危险因素,并比较了接受或未接受抗血管生成药物(AA)治疗的转移性肾细胞癌(mRCC)中脑转移的发生率。

方法

回顾了1995年至2008年在法国一家癌症中心接受治疗的所有连续性转移性肾细胞癌患者的数据。患者在转移诊断时经组织学证实为晚期肾细胞癌且无同步脑转移。抗血管生成药物包括索拉非尼、舒尼替尼和贝伐单抗。我们还纳入了接受mTor抑制剂替西罗莫司和依维莫司治疗的患者,因为它们也具有抗血管生成活性。采用Fisher精确检验比较接受或未接受抗血管生成药物治疗的两组患者的特征。采用Kaplan-Meier法探讨抗血管生成药物对总生存期(OS)和脑转移累积发生率(CRBM)的影响。

结果

共确定199例晚期肾细胞癌患者,51例接受抗血管生成药物治疗,148例未接受抗血管生成药物治疗。中位随访时间为40个月。35例患者发生脑转移。接受抗血管生成药物治疗组和未接受抗血管生成药物治疗组之间的特征不均衡,抗血管生成药物治疗组的预后因素更好。中位总生存期为24个月。抗血管生成药物治疗与较低的脑转移累积发生率无关(风险比=0.58[0.26-1.30],P=0.187)。未接受抗血管生成药物治疗组无脑转移的中位生存期为11.8个月,95%置信区间(4.95-18.65),抗血管生成药物治疗组为28.9个月,95%置信区间(18.64-39.16)。碱性磷酸酶(AP)是脑转移的独立预后因素(P=0.05)。在多变量Cox模型中,调整碱性磷酸酶后,抗血管生成药物并未改善脑转移累积发生率(调整后风险比=0.53[0.22-1.32])。

结论

在这项回顾性研究中,抗血管生成药物并未显著降低脑转移累积发生率。碱性磷酸酶升高是转移性肾细胞癌脑转移的预测因素。

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